U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 82

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5351734translocation1nstd200human GRCh38 chr3: 46,499,780-46,499,780 , GRCh38 chr3: 46,499,859-46,499,859 , GRCh37.p13 chr3: 46,541,349-46,541,349 , GRCh37.p13 chr3: 46,541,270-46,541,270 RTP3
    nsv5338780translocation1nstd200human GRCh37 chr3: 46,541,270-46,541,270 , GRCh37 chr3: 46,541,349-46,541,349 , GRCh38.p12 chr3: 46,499,859-46,499,859 , GRCh38.p12 chr3: 46,499,780-46,499,780 RTP3
    nsv5211169copy number variation1nstd204human GRCh37.p13 chr3: 46,500,291-46,685,390 , GRCh38.p13 chr3: 46,458,801-46,643,900 LTF, CRIPTO, 4 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924391copy number variation1nstd200human GRCh38 chr3: 46,500,315-46,500,521 , GRCh37.p13 chr3: 46,541,805-46,542,011 RTP3
    nsv4924390copy number variation1nstd200human GRCh38 chr3: 46,433,915-46,659,110 , GRCh37.p13 chr3: 46,475,406-46,700,600 LTF, CRIPTO, 4 more genes
    nsv4911118copy number variation1nstd200human GRCh38 chr3: 46,420,758-46,510,692 , GRCh37.p13 chr3: 46,462,249-46,552,182 RTP3, LTF, 1 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4793958copy number variation1nstd200human GRCh37 chr3: 46,500,364-46,685,484 , GRCh38.p12 chr3: 46,458,874-46,643,994 LTF, LRRC2-AS1, 4 more genes
    nsv4727980copy number variation1nstd197human GRCh37 chr3: 46,399,020-46,569,071 , GRCh38.p12 chr3: 46,357,529-46,527,581 CCR5, LTF, 6 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4378611copy number variation1nstd173human GRCh37 chr3: 46,462,849-46,549,188 , GRCh38.p12 chr3: 46,421,358-46,507,698 LTF, RTP3, 1 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4091326copy number variation1nstd166human GRCh37.p13 chr3: 46,541,270-46,541,349 , GRCh38.p12 chr3: 46,499,780-46,499,859 RTP3
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 RBM5-AS1, PRSS42P, 185 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 ACAA1, ACVR2B, 344 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center